Computerized determination of insulin pump therapy parameters using real time and retrospective data processing

ABSTRACT

Methods and devices for providing computerized adjustment to therapy parameters using real time and retrospective data processing is provided. Embodiments include receiving a respective data set from an infusion device and an analyte monitoring device for a predetermined time duration, user notification and reminder of the predetermined time duration, time synchronizing the received respective data set, detecting one or more marked data from the one or more respective data set received, establishing one or more filtering criteria to filter of retrospective or historical data based on certain condition, performing automated data analysis based on the detected one or more marked data or the data achieving certain predetermined condition to generate a modification to a therapy profile, generating and modifying rules for profile modification, and providing the generated modification to the therapy profile for reporting and transmission.

BACKGROUND

Diabetic patients typically administer insulin to sustain their physiological conditions. Typically, these patients administer doses of either fast acting or slow acting insulin using needle type syringes, for example, prior to meals, and/or at a suitable time during the course of each day contemporaneously with the blood glucose level testing using fingerstick blood glucose testing, for example. If insulin is not suitably administered, the diabetic patients risk serious if not fatal damage to the body.

Continued development and improvement in the external infusion pump therapy in recent years have drawn much appeal to the diabetic patients for, among others, improved management of diabetes by better regulating and controlling the intake of insulin. Typically, the patient inserts a cannula which is connected to as infusion tubing attached to an external pump, and insulin is administered based on a preprogrammed basal profiles. Moreover, the external infusion devices presently available include computational capability to determined suitable bolus doses such as carbohydrate bolus and correction bolus, for example, to be administered in conjunction with the infusion device executing the patient's basal profile.

Commercially available infusion devices such as insulin pumps are programmable and include sophisticated functionalities to enhance therapy management. Consistent with the sophistication of these devices, it is often cumbersome and trying to program these complex devices to the desired delivery, notification, modification and/or other adjustments or settings to be suitable for each user's physiology or therapy.

Programming such infusion devices require the entry of many variables and parameters, some of which are entered or provided into the device based, at least in part on the knowledge or experience of the user and/or the healthcare provider. For example, to modify one or more basal delivery settings, the infusion device user may use prior knowledge based on past experience, in addition to subjectively determined parameters, for example, the time period for inputting measurement values of the blood glucose level when determining a correction bolus amount.

It goes without saying for diabetics on insulin pump therapy, continual refinement of the basal insulin delivery rate, insulin to carbohydrate ratio determination, insulin sensitivity level, duration of insulin action, to name a few, are important in achieving successful therapy management. Often times, however, the refinement process is complex and iterative.

SUMMARY

Embodiments of the subject disclosure include methods device for programming a therapy delivery device such as a medication infusion device including, for example insulin pump. More particularly, embodiments of the present disclosure include receiving a respective data set from an infusion device and an analyte monitoring device for a predetermined time duration, time synchronizing the received respective data set, detecting one or more marked data from the one or more respective data set received, performing automated data analysis based on the detected one or more marked data or data filters to generate a modification to a therapy profile, and providing the generated modification to the therapy profile.

Also provided are systems, computer program products, and kits.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows a block diagram of an overall computerized adjustment to therapy parameters using real time and retrospective data processing in accordance with one aspect;

FIG. 2 is a flowchart illustrating a routine for computerized adjustment to therapy parameters using real time and retrospective data processing in accordance with one aspect of the present disclosure; and

FIGS. 3-14 are screen shot illustrations of the overall computerized adjustment to therapy parameters using real time and retrospective data processing in accordance with one aspect of the present disclosure.

DETAILED DESCRIPTION

Within the scope of the present disclosure, there are provided method and system for providing automated or semi-automated computerized adjustment to therapy parameters using real time and retrospective data processing including device and/data synchronization, bi-directional communication, data storage and processing, as well as providing a robust user interface. Embodiments of the present disclosure include predetermined time period for data collection including data related to monitored analyte levels, infusion device delivery characteristics, and events markers, if any associated with the user. Upon expiration of the data collection period, the information is uploaded to a data management and analysis tool which, in one embodiment, may be configured to automatically initiate processing of the received data, including, detecting data marked or identified for performing automatic or semi-automatic adjustment, and output or generate a recommended refinement to the therapy profile, for example, which is then output to the user or the healthcare provider or directly programmed into the therapy delivery device.

Before the present disclosure is described in additional detail, it is to be understood that this disclosure is not limited to particular embodiments described, as such may, of course, vary. It is also to be understood that the terminology used herein is for the purpose of describing particular embodiments only, and is not intended to be limiting, since the scope of the present disclosure will be limited only by the appended claims.

Where a range of values is provided, it is understood that each intervening value, to the tenth of the unit of the lower limit unless the context clearly dictates otherwise, between the upper and lower limit of that range and any other stated or intervening value in that stated range, is encompassed within the disclosure. The upper and lower limits of these smaller ranges may independently be included in the smaller ranges is also encompassed within the disclosure, subject to any specifically excluded limit in the stated range. Where the stated range includes one or both of the limits, ranges excluding either or both of those included limits are also included in the disclosure.

Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this disclosure belongs. Although any methods and materials similar or equivalent to those described herein can also be used in the practice or testing of the present disclosure, the preferred methods and materials are now described. All publications mentioned herein are incorporated herein by reference to disclose and describe the methods and/or materials in connection with which the publications are cited.

It must be noted that as used herein and in the appended claims, the singular forms “a”, “an”, and “the” include plural referents unless the context clearly dictates otherwise.

The publications discussed herein are provided solely for their disclosure prior to the filing date of the present application. Nothing herein is to be construed as an admission that the present disclosure is not entitled to antedate such publication by virtue of prior disclosure. Further, the dates of publication provided may be different from the actual publication dates which may need to be independently confirmed.

As will be apparent to those of skill in the art upon reading this disclosure, each of the individual embodiments described and illustrated herein has discrete components and features which may be readily separated from or combined with the features of any of the other several embodiments without departing from the scope or spirit of the present disclosure.

The figures shown herein are not necessarily drawn to scale, with some components and features being exaggerated for clarity.

FIG. 1 shows a block diagram of an overall therapy delivery device programming tool in accordance with one aspect of the present disclosure. Referring to the Figure, the system for providing automated or semi-automated computerized adjustment to therapy parameters using real time and retrospective data processing 100 includes a therapy delivery device 110 such as an insulin delivery device capable of data communication with a controller unit 120 and a data processing terminal 130. Also shown in an analyte monitoring system 140 configured for communication with the controller unit 120 and the data processing terminal 130. In aspects of the present disclosure, the analyte monitoring system 140 may be configured to communicate directly with the therapy delivery device 110.

Within the scope of the present disclosure, two or more of the components shown in the system 100 of FIG. 1 may be integrated into a single device or housing. For example, the insulin delivery device 110 and the analyte monitoring system 140 may be provided in a single integrated device housing while maintaining the separate functionality of medication delivery and analyte monitoring, respectively.

The therapy delivery device 110 in one embodiment may include an external infusion device such as an external insulin pump, an implantable infusion device, an on-body micropump device, a transdermal delivery device, or any other suitable microprocessor controlled medication delivery device. Furthermore, the analyte monitoring system 140 may include, one or more transcutaneous analyte sensors such as glucose sensors configured for fluid contact with an analyte of a user for a predetermined time period such as for example, approximately five days, seven days or more.

Referring back to FIG. 1, the controller unit 120 may be configured in one aspect to perform some or all of the control functions associated with the operation of the insulin delivery device 110 and/or the analyte monitoring system 140. In another aspect, the control functions and operations provided to the controller unit 120 may be to provide redundancy in operation, such that the same operations and/or control functions may be provided in the respective insulin delivery device 110 and/or the analyte monitoring system 140.

In one aspect, the therapy delivery device 110 may include one or more user interface components such as a display, input buttons, speakers for providing audible or audio output, and the like. In one aspect, the therapy delivery device 110 may be an ambulatory device and configured to be carried around by the user. In still a further aspect, the therapy delivery device 110 may include a communication component which allows the device 110 to connect to or communicate with one or more of the controller unit 120 and the data processing terminal 130. The communication link between the therapy delivery device 110 and the one or more of the controller unit 120 and the data processing terminal 130 may include RF communication, Infrared communication, 801.x1 based communication protocol, cellular network based communication protocol and the like. In accordance with aspects of the present disclosure, the communication between the various components of the overall system 100 shown in FIG. 1 may also includes wires connection using, for example, USB connection, RS-232 connection, or any other suitable data transfer connection.

In one aspect, the therapy delivery device 110 may be configured to deliver medication such as insulin using an infusion set connectable to the housing of the device and in fluid communication with one or more reservoirs housed within the device 110, where the infusion set includes a cannula for medication delivery to the user or patient. In a further aspect, the therapy delivery device 110 is microprocessor driven and controlled by one or more microprocessor units to execute functions related to the medication delivery, operational condition monitoring of the therapy delivery device, and the like.

Referring back to FIG. 1, also shown is the controller unit 120 which may include a wireless or wired communication device which is configured to control at least in part, the operation of the therapy delivery device, and further, configured to communicate with the data processing terminal 130. Each communication link between the various components shown in FIG. 1 including the therapy delivery device 110, the controller unit 120, and the data processing terminal 130 may be bidirectional. In one aspect, the controller unit 120 may include some or all of the functionalities provided in the therapy delivery device 110 including the control of the medication dispensing protocol, condition notification such as detected occlusion in the infusion tubing, and/or along the fluid path from the therapy delivery device 110 to the user, programming, controlling or monitoring the operation of the therapy delivery device 110.

Optionally, the controller unit 120 may include a strip port for receiving an in vitro blood glucose test strip for determining a blood glucose measurement. Additionally, the controller unit 120 may include the functionalities of an analyte monitoring device which may be configured to be in communication with an analyte sensor for monitoring an analyte level of a user. Further detailed descriptions of embodiments of the continuous analyte monitoring system, embodiments of its various components are provided in U.S. Pat. No. 6,175,752 issued Jan. 16, 2001 entitled “Analyte Monitoring Device and Methods of Use”, and in application Ser. No. 10/745,878 filed Dec. 26, 2003 entitled “Continuous Glucose Monitoring System and Methods of Use”, each assigned to the Assignee of the present application, disclosure of each of which are incorporated by reference for all purposes.

Referring back to FIG. 1, the data processing terminal 130 in one aspect may include a personal computer, a portable computer such as a laptop or a handheld device (e.g., personal digital assistants (PDAs), telephones such as a cellular phones (e.g., a multimedia and Internet-enabled mobile phone such as an iPhone or a Blackberry device), mp3 players, pagers, and the like), each of which may be configured for data communication with the delivery device 110 and/or the controller unit 120 via wired or wireless connection. Additionally, the data processing terminal 130 may further be connected to a data network (not shown) for storing, retrieving, updating, and/or analyzing data associated with the therapy delivery device 110 as well as the controller unit 120.

In this manner, in accordance with aspects of the present disclosure, data collected or monitored by the insulin delivery device 110, the controller unit 120 and/or the analyte monitoring system 140 is provided to the data processing terminal 130 which in turn, may be configured to perform, automatically or semi-automatically, processing of the collected and received data, to modify the therapy management profile to recommend to the user and for execution by the insulin delivery 110 to improve glycemic control. That is, in one aspect, the data processing terminal 130 may be configured to include software or programming to receive data associated with insulin delivery and time corresponding monitored analyte levels from the delivery device 110 and the analyte monitoring system 140, respectively, and automatically or semi-automatically, with one or more user inputs or prompts, execute data analysis and therapy recommendation procedure or routine.

FIG. 2 is a flowchart illustrating a routine for computerized adjustment to therapy parameters using real time and retrospective data processing in accordance with one aspect of the present disclosure. Referring to the Figure, after a predetermined time has elapsed, the data processing terminal 130 may be configured to initiate communication with the devices in the overall system including, for example insulin delivery device 110, the controller unit 120 and the analyte monitoring system 140 (210). The predetermined time period may be programmable and based on, for example, a time window that is sufficiently wide to provide meaningful data for analysis and processing to determine fine tuning of the therapy profile or patient achieving certain targeted events as prescribed by the physician.

In one aspect, the communication between the data processing terminal 130 and the devices in the system 100 may not be initiated by the data processing terminal 140, but rather, established at different time periods when each of the insulin delivery device 110, the controller unit 120 and the analyte monitoring system 140 is within communication range with the data processing terminal 140, and which may include overlapping but not identical time periods for each communication from the various devices to the data processing terminal 140. In such as case, it is important to have the clocks or timing components in each device in the system 100 to be synchronized, such that the data processing terminal 130 may accurately correlate the information received from each device. That is, the time base for data or information from each device in the system may be synchronized to provide meaningful and accurate data.

Referring to FIG. 2, with the communication link established, the time based data from each device is received or collected for example, representative of the time period or predetermined time period identified by the data processing terminal 130 (FIG. 1) for analysis (220). The data processing terminal 130 may be further configured to detect data marked for fining tuning (230) based on preliminary analysis of information received from each device. For example, instances of hypoglycemia and/or hyperglycemia detection from the analyte monitoring system 140, ingesting of prescribed meal and its impact on the subsequent detected rate of change of the analyte level, detected rate of change of the analyte levels that deviate beyond a predefined level of tolerance, and the like, which events are correspondingly marked by the respective devices such as the analyte monitoring system 140 and identified as part of the data transfer from the analyte monitoring system 140 to the data processing terminal 130.

Similarly, data from the insulin delivery device 110 may be marked by the device during the course of the medication delivery, and thereafter provided to the data processing terminal 130. Examples of such marked data may include, but is not limited to, time information associated with user administered bolus doses, execution of temporary basal and delivery profiles for the same, bolus insulin amount and its impact on the subsequent rate of change of analyte level, compliance or noncompliance to alarm or alert conditions, and the like. In one aspect, the insulin delivery device 110 may be programmed to detect occurrence of such event and identify data or information associated with the detection of such occurrences and subsequently to provide that information in addition to the associated data to the data processing terminal 130.

Referring back to FIG. 2, in one aspect, the data processing terminal 130 (FIG. 1) is configured to perform one or more processes or routines to analyze the detected marked data and associated information received from the insulin delivery device 110, the controller unit 120 and the analyte monitoring system 140 (240). After processing the detected marked data and associated information, the data processing terminal 130 may be configured to generate a therapy modification output that refines or fine tunes the one or more aspect of the therapy management associated with the marked data or unmarked data if they meet certain prescribed filtering criteria (250). In one aspect, the generated therapy modification as well as the underlying processing may be performed automatically by the data processing terminal 130 upon detection of the communication link with the one or more devices in the system 100. Alternatively, within the scope of the present disclosure, the analysis and fine tuning of the therapy profile may be initiated based on user prompt or command, or upon detection of a predetermined time period for which data from the various devices and components have been received so as to provide a meaningful analysis based on marked data and associated information.

FIGS. 3-14 are screen shot illustrations of the overall computerized adjustment to therapy parameters using real time and retrospective data processing in accordance with one aspect of the present disclosure. As shown in the Figures, during data connection and processing, the status information as well as user inputtable parameters are displayed in one embodiment as visual representation to the user. For example, FIG. 3 shows a status screen during data collection or synchronization with the delivery device 110 including, for example, search and verification of any data marked (for example, the basal test marker events shown). As can be further seen from FIGS. 3-14, during the data collection, synchronization and processing routines, the data processing terminal 130 may be configured to provide a step by step visual presentation of the information being processed and various routines being executed, and optionally request user input or confirmation.

In another aspect, the data processing terminal 130 may be programmed with one or more predefined filter functions and configured to identify relevant segments of retrospective or historical data that can be used for further analysis.

Accordingly, one embodiment of the present disclosure includes receiving a respective data set from an infusion device and an analyte monitoring device for a predetermined time duration, time synchronizing the received respective data set, detecting one or more marked data from the one or more respective data set received, performing automated data analysis based on the detected one or more marked data to generate a modification to a therapy profile, and providing the generated modification to the therapy profile.

The data set from the infusion device includes an executed medication delivery profile associated with the predetermined time duration.

The data set from the analyte monitoring device includes monitored analyte level associated with the predetermined time duration.

Time synchronizing the received respective data set includes aligning the time information of each data set based on a common time base.

In one aspect, the detected one or more marked data includes an indication of a hypoglycemic event, a hypoglycemic event, a rate of change of analyte level exceeding a predetermined threshold level, therapy compliance information, missed analyte sensor calibration event, missed meal bolus event, frequency alarm event, and frequency of alert event.

Further, performing the automated data analysis includes refining an executed therapy profile based at least in part in the data processing associated with the marked data and related information.

Also, in one aspect, the automated data analysis is initiated in response to the detection of the marked data.

Also, in another respect, the automated data analysis may be initiated in response to the data achieving a preset number of prescribed events to proceed with meaningful analyses.

Moreover, in a further aspect, the therapy profile includes insulin therapy profile.

Additionally included in a further embodiment is transmitting the generated modification to the therapy profile in response to a received confirmation.

An apparatus in accordance with another aspect includes a data communication interface, one or more processors operatively coupled to the data communication interface, a memory for storing instructions which, when executed by the one or more processors, causes the one or more processors to receive a respective data set from an infusion device and an analyte monitoring device for a predetermined time duration, time synchronize the received respective data set, detect one or more marked data from the one or more respective data set received, perform automated data analysis based on the detected one or more marked data to generate a modification to a therapy profile, and provide the generated modification to the therapy profile.

Moreover, one or more storage devices having processor readable code embodied thereon, said processor readable code for programming one or more processors to fine tune therapy profile in accordance with still another aspect may include receiving a respective data set from an infusion device and an analyte monitoring device for a predetermined time duration, time synchronizing the received respective data set, detecting one or more marked data from the one or more respective data set received, performing automated data analysis based on the detected one or more marked data to generate a modification to a therapy profile, and providing the generated modification to the therapy profile.

The various processes described above including the processes performed by the delivery device 110, the controller unit 120, the analyte monitoring system 140, and the data processing terminal 130 (FIG. 1) in the software application execution environment in the overall system for providing delivery device programming tool 100 including the processes and routines described in conjunction with FIG. 2, may be embodied as computer programs developed using an object oriented language that allows the modeling of complex systems with modular objects to create abstractions that are representative of real world, physical objects and their interrelationships. The software required to carry out the inventive process, which may be stored in the memory or storage device (not shown) of the delivery device 110, the controller unit 120, the data processing terminal 130, and the analyte monitoring system 140 may be developed by a person of ordinary skill in the art and may include one or more computer program products.

Various other modifications and alterations in the structure and method of operation of this disclosure will be apparent to those skilled in the art without departing from the scope and spirit of the embodiments of the present disclosure. Although the present disclosure has been described in connection with particular embodiments, it should be understood that the present disclosure as claimed should not be unduly limited to such particular embodiments. It is intended that the following claims define the scope of the present disclosure and that structures and methods within the scope of these claims and their equivalents be covered thereby. 

What is claimed is:
 1. A method, comprising: receiving a respective data set from an infusion device and an analyte monitoring device for a predetermined time duration; time synchronizing the received respective data set; detecting one or more marked data from the one or more respective data set received; performing automated data analysis based on the detected one or more marked data to generate a modification to a therapy profile; and providing the generated modification to the therapy profile.
 2. The method of claim 1 wherein the data set from the infusion device includes an executed medication delivery profile associated with the predetermined time duration.
 3. The method of claim 1 wherein the infusion device is configured to notify a user that the predetermined time duration is in effect.
 4. The method of claim 1 including performing the automated data analysis based on detection of the occurrence of a preset number of events and/or conditions in the respective data set to generate the modification to the therapy profile.
 5. The method of claim 4 including providing user formulation tools to modify one or more rules or guidelines for therapy modification.
 6. The method of claim 1 wherein the data set from the analyte monitoring device includes monitored analyte level associated with the predetermined time duration.
 7. The method of claim 1 wherein the analyte monitoring device is configured to notify a user that the predetermined time duration is in effect.
 8. The method of claim 1 wherein time synchronizing the received respective data set includes aligning a time of event occurrence information for associated events of each data set based on a common time base.
 9. The method of claim 1 wherein the detected one or more marked data includes an indication of a meal event, exercise event, drug ingestion event, health state event, hypoglycemic event, hyperglycemic event, rate of change of analyte level exceeding a predetermined threshold level, therapy compliance information, missed analyte sensor calibration event, missed meal bolus event, frequency alarm event, and frequency of alert event.
 10. The method of claim 1 wherein performing the automated data analysis includes refining an executed therapy profile based at least in part in the data processing associated with the marked data and related information.
 11. The method of claim 1 wherein performing the automated data analysis includes refining an executed therapy profile based at least in part in the data processing associated with a pre-defined filter criteria of unmarked data.
 12. The method of claim 1 wherein the automated data analysis is initiated in response to the detection of the marked data.
 13. The method of claim 1 wherein the automated data analysis is initiated in response to the data achieving a preset number of pre-defined events or conditions.
 14. The method of claim 1 wherein the therapy profile includes insulin therapy profile, glucose alarm settings, target blood glucose profile, carbohydrate ratio profile or insulin sensitivity profile.
 15. The method of claim 1 including transmitting the generated modification to the therapy profile in response to a received confirmation.
 16. The method of claim 1 including generating or modifying one or more rules for generating therapy profile modification.
 17. An apparatus, comprising: a data communication interface; one or more processors operatively coupled to the data communication interface; and a memory for storing instructions which, when executed by the one or more processors, causes the one or more processors to receive a respective data set from an infusion device and an analyte monitoring device for a predetermined time duration, time synchronize the received respective data set, detect one or more marked data from the one or more respective data set received, perform automated data analysis based on the detected one or more marked data to generate a modification to a therapy profile, and provide the generated modification to the therapy profile.
 18. The apparatus of claim 17 wherein the data set from the infusion device includes an executed medication delivery profile associated with the predetermined time duration.
 19. The apparatus of claim 17 wherein the memory for storing instructions which, when executed by the one or more processors causes the one or more processors to issue one or more notification to perform or prohibit performance of one or more user based events during the predetermined time period.
 20. The apparatus of claim 17 wherein the respective data set received from the analyte monitoring device includes monitored analyte level associated with the predetermined time duration.
 21. The apparatus of claim 17 wherein the memory for storing instructions which, when executed by the one or more processors, causes the one or more processors to align the time information of each data set based on a common time base.
 22. The apparatus of claim 17 wherein the detected one or more marked data includes an indication of a meal event, exercise event, drug ingestion event, health state event, hypoglycemic event, hyperglycemic event, rate of change of analyte level exceeding a predetermined threshold level, therapy compliance information, missed analyte sensor calibration event, missed meal bolus event, frequency alarm event, and frequency of alert event.
 23. The apparatus of claim 17 wherein the memory for storing instructions which, when executed by the one or more processors, causes the one or more processors to refine an executed therapy profile based at least in part in the data processing associated with the marked data and related information.
 24. The apparatus of claim 17 wherein the memory for storing instructions which, when executed by the one or more processors, causes the one or more processors to refine an executed therapy profile based at least in part in the data processing associated with a pre-defined filter criteria of unmarked data.
 25. The apparatus of claim 17 wherein the automated data analysis is initiated in response to the detection of the marked data.
 26. The apparatus of claim 17 wherein the therapy profile includes insulin therapy profile, glucose alarm settings, target blood glucose profile, carbohydrate ratio profile, or insulin sensitivity profile.
 27. The apparatus of claim 17 wherein the memory for storing instructions which, when executed by the one or more processors, causes the one or more processors to transmit the generated modification to the therapy profile in response to a received confirmation.
 28. The apparatus of claim 17 wherein the memory for storing instructions which, when executive by the one or more processors, causes the one or more processors to update one or more rules for generating therapy profile modification.
 29. One or more storage devices having processor readable code embodied thereon, the processor readable code for programming one or more processors to fine tune therapy profile, comprising: receiving a respective data set from an infusion device and an analyte monitoring device for a predetermined time duration; time synchronizing the received respective data set; detecting one or more marked data from the one or more respective data set received; performing automated data analysis based on the detected one or more marked data to generate a modification to the therapy profile; and providing the generated modification to the therapy profile. 